Emanuela Dazzo

发表

The novel S59P mutation in the TNFRSF1A gene identified in an adult onset TNF receptor associated periodic syndrome (TRAPS) constitutively activates NF-κB pathway

P. Tighe, O. Negm, L. Punzi, 2015, Arthritis Research & Therapy.

A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signalling and miRNA dysregulation

G. Lembo, P. Braghetta, P. Bonaldo, 2018, Cardiovascular research.

LGI1 tumor tissue expression and serum autoantibodies in patients with primary malignant glioma

R. Michelucci, C. Nobile, Emanuela Dazzo, 2018, Clinical Neurology and Neurosurgery.

The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations

P. Striano, R. Michelucci, O. Mecarelli, 2017, Epilepsy & Behavior.

Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26

A. Giallonardo, J. Fattouch, Alessandro Spadotto, 2014, Epilepsy Research.

Desmin Mutations and Arrhythmogenic Right Ventricular Cardiomyopathy

G. Thiene, C. Basso, M. Calore, 2013, The American journal of cardiology.

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy

P. Striano, R. Michelucci, A. Gambardella, 2015, Epilepsia.

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations

P. Striano, R. Michelucci, Marco Marchini, 2013, Epilepsia.

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy.

Paco Hulpiau, Andrea Nava, D. Corrado, 2013, European heart journal.

Pericentriolar material analyses in normal esophageal mucosa, Barrett's metaplasia and adenocarcinoma.

Maria Pia Vitale, M. Rugge, M. Fassan, 2010, Histology and histopathology.

Genetics of Epilepsy and Relevance to Current Practice

R. Michelucci, C. Nobile, Emanuela Dazzo, 2012, Current Neurology and Neuroscience Reports.

CDX2 hox gene product in a rat model of esophageal cancer

M. Rugge, M. Fassan, G. Ingravallo, 2009, Journal of experimental & clinical cancer research : CR.

Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.

Silvio C. E. Tosatto, P. Striano, R. Michelucci, 2015, American journal of human genetics.

Selection of multipotent cells and enhanced muscle reconstruction by myogenic macrophage-secreted factors.

C. Romualdi, P. de Coppi, L. Vitiello, 2009, Experimental cell research.

Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy

D. Corrado, G. Thiene, C. Basso, 2013, European Journal of Human Genetics.

CNTNAP2 mutations and autosomal dominant epilepsy with auditory features

Silvio C. E. Tosatto, R. Michelucci, S. Tosatto, 2018, Epilepsy Research.

Secretion-Positive LGI1 Mutations Linked to Lateral Temporal Epilepsy Impair Binding to ADAM22 and ADAM23 Receptors

Silvio C. E. Tosatto, S. Tosatto, L. Vitiello, 2016, PLoS genetics.

Autosomal dominant lateral temporal epilepsy (ADLTE): Novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras

P. Striano, C. Millino, B. Pacchioni, 2015, Epilepsy Research.

Mutations in MICAL‐1cause autosomal‐dominant lateral temporal epilepsy

P. Striano, R. Michelucci, R. Pasterkamp, 2018, Annals of neurology.

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy.

D. Corrado, G. Thiene, C. Basso, 2013, European heart journal.

Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture

I. Scheffer, P. Striano, P. Kwan, 2023, Annals of neurology.